P. gingivalis vaccine

ABSTRACT

A vaccine composition is provided which comprises a rag nucleic acid sequence for the prevention and/or treatment of infection by  P. gingivalis . Uses of such nucleic acid sequences, proteins coded for by such sequences and antibodies raised against such proteins in medicine are also provided. Kits for the detection of  P. gingivalis  in a sample are also provided.

The present invention relates to a vaccine, which is a complex of all possible outer membrane protein alleles of RagB of Porphyromonas gingivalis, and uses of the vaccine to prevent or treat periodontitis caused from different P. gingivalis strains.

Periodontal disease is an inflammatory, infectious condition of the soft and hard tissues, which secure the teeth in the mouth. The inflammatory process is driven by a microbial challenge presented by subgingival plaque microorganisms. It is now accepted that Porphyromonas gingivalis is a major periodontopathogenic organism which is particularly relevant in the aetiology of adult periodontal disease (2) (10) (14) (17) (26) (36) (39) (45).

Analysis of the microbiology of subgingival plaque in periodontal disease has revealed a very complex mixture of genera and species. However, in recent years, cluster analysis of DNA:DNA checkerboard data and correlation with the clinical status of the sample site from large scale clinical studies involving >16,000 samples by Socransky and colleagues at the Forsyth Institute in Boston USA has revealed that destructive disease is very strongly associated with just three organisms: P. gingivalis, Treponema denticola and Bacteroides forsythus (Tannerella forsythensis) (9) (16) (46) (47) (49).

Genome sequence of Porphyromonas gingivalis strain W83 has been completed (33). However, genotypic characterization of P. gingivalis strains has revealed extensive heterogeneity in natural populations of this bacterium (3) (12) (15) (23) (25) (28) (30) (35) (37) (56). The development of a vaccine for periodontal disease based on surface and extracellular antigens of P. gingivalis has been pursued by several groups worldwide. Cysteine proteases (gingipains), capsular polysaccharide and fimbriae have all been considered (13) (29) (34) (40) (43) (53) (55). However to date few of these studies have addressed the problems of strain variation and the applicability of a single vaccine strategy to counter either allelic variation or post-translational effects caused by variable glycosylation (7).

Current periodontal disease treatment relies upon mechanical debridement, antibiotics and surgery.

Approximately 10-15% of most populations exhibit one of the destructive forms of periodontal disease in the UK. The prevalence of these diseases is reflected in the direct financial costs of treatment, which in 2000/1 were estimated to be £230 million by the National Health Service in England and Wales (Dental Practice Board Annual Report 2001-02). However these costs only apply to actual periodontal treatments provided by general dental practitioners within the NHS general dental services and therefore excludes specialist treatment, any treatment provided by community services and hospital services, any treatment provided privately, and does not include costs associated with treating the consequences of periodontal treatment for example x-rays, detailed examinations, dentures, bridges, extractions and so on. Hence the actual costs to the NHS of treating the consequences of the disease in England and Wales are probably in excess of £500 million and this excludes hospital services or private health care expenditure. The increasing life expectancy in the population and conservation of more standing teeth into later life, due to caries control, will inevitably lead to an increasing number of treatment courses and hence public health costs will continue to rise.

Furthermore there is now increasing evidence to suggest that the persistent, Gram-negative infections of the periodontal tissues, which typify these diseases, may have more serious consequences on the general health of the affected individual. Whilst the extent of the problem remains controversial, periodontal disease is emerging as a significant risk factor for cardiovascular disease and in the case of pregnant women for an increased risk of giving birth to a premature low birth weight baby.

Periodontal diseases are endemic in all populations and are a major under-served medical market. In the US, 40% of the adult population suffer at least a mild form of the disease and total expenditure on periodontal and preventative procedures in 1999 in the US were $14.3 billion.

There are a number of stages in the progression of periodontitis at which methods of disease control can be applied. Current treatments e.g. antisepsis or surgical treatment have shortfalls in efficacy. Effective dental plaque control can prevent and control gingivitis and periodontitis. Mechanical plaque control, i.e. tooth brushing, is the first line of defence but is generally of variable quality, depending on individual, societal and cultural factors.

Chemical control of dental plaque includes the use of antimicrobial agents, such as triclosan, chlorhexidine and sodium hypochlorite, which are available for self-administration through a variety of vehicles, most commonly mouthwash preparations. This method of plaque control requires regular user compliance, is relatively costly and has limited accessibility subgingivally and interproximally.

Antibiotic therapy of periodontitis includes the use of metronidazole, clindamycin and ciprofloxacin. The widespread use of such compounds in the prevention of gum disease is unlikely due to potential problems with strain resistance, adverse host reaction and secondary infection.

Other recent developments in the therapy of bacterially mediated oral diseases include the use of an antibody that binds specifically to S. mutans, a major cause of tooth decay. This antibody is intended for regular topical preventative administration by dentists and patients. Pre-clinical animal studies have demonstrated an antibacterial effect and decay prevention.

A variety of immuno-modulatory strategies have been devised and applied to control oral bacteria. These include passive immunisation using a humanised sIgA antibody originally derived from a mouse IgG monoclonal antibody (1) (6) (27), immunisation of primates with a key antigen of the target organism (11) (21) (24) (51), the use of peptides corresponding to key functional domains of the target antigen (22) (31) (50), delivery of the antigen of the target organism as a recombinant protein expressed in an oral commensal bacterium (42). Hence there is significant state of the art in this area and application of these methodologies could also be applied to the generation of an immune response to the RagB antigen.

At present there are no vaccines or products, either marketed or in development, which are targeted at all P. gingivalis strains for the prevention of periodontitis.

Current treatment of periodontal diseases is, in the US at least, largely a hi-tech, private market. There is therefore a need for a vaccine that is cheaper, easily administered (through a range of commercial products such as toothpastes and mouthwash) and accessible to a much wider global population. It is also important that any vaccine treatment is effective against all common strains of the pathogen.

The present invention provides a solution to these problems in the form of an effective vaccine comprising all the major RagB forms of P. gingivalis, which would prevent periodontal disease by stopping infection by this organism and from infection caused by different P. gingivalis strains.

According to a first aspect of the invention, there is provided a vaccine composition constituted from nucleic acid molecules having a sequence of nucleotides 1-1518 of QMLragB SEQ.ID.NO:5, nucleotides 1-1506 of ThairagB SEQ.ID.NO:6, nucleotides 1-1506 of W50ragB SEQ.ID.NO:7, and nucleotides 1-1518 381ragB SEQ.ID.NO:8 or a fragment thereof.

The nucleic acid molecule may have a sequence of a combination of the nucleic acid sequences of nucleotides 1-1518 of SEQ.ID.NO:5 (QMLragB), nucleotides 1-1506 of SEQ.ID.NO:6 (ThairagB), nucleotides 1-1506 of SEQ.ID.NO:7 (W50ragB) and nucleotides 1-1518 SEQ.ID.NO:8 (381ragB). For example, the nucleic acid sequence may have a sequence of the nucleic acid sequences of SEQ.ID.NO:5 and SEQ.ID.NO:6, or the nucleic acid sequences of SEQ.ID.NO:5, SEQ.ID.NO:6, SEQ.ID.NO:7 and SEQ.ID.NO:8, or a fragment thereof.

Vaccine compositions according to the present invention may be formulated and adapted for any convenient route of administration, such as oral, inhalation, intravenous injection, or intramuscular injection routes.

The vaccines may comprise additional pharmaceutically acceptable excipients or diluents as required.

To be effective, a vaccine must induce long-standing immunity that acts at the appropriate body sites and against the appropriate microbial antigens to prevent disease in all persons at risk; to be practical, it must also be safe, inexpensive, and easy to store and administer.

Some useful vaccines may comprise live, naturally occurring microbes that share important antigens with a pathogen but are not pathogenic themselves; other vaccines are prepared from potentially pathogenic bacteria or viruses that have either been killed or are attenuated; certain vaccines are made of purified macromolecules, for example proteins or glycoproteins; and other strategies for immunization rely on the use of DNA, RNA, etc.

A preferred vaccine of the present invention may be based on a vaccine delivery system for oral colonization and immune response to P. gingivalis using live bacteria suitable for this purpose. The possible candidate vectors are Bacillus subtilis spores (8) (18), Streptococcus gordonii(44) (41) and Bordetella bronchiseptica (48).

The vaccines of the present invention may also contain adjuvant substances to assist where necessary if the vaccine is composed of purified antigen. Any suitable pharmaceutically acceptable adjuvant may be used as appropriate, for example, aluminium salts, fragments of bacterial cell wall (e.g. Freund's adjuvant), killed bacteria, bacterial polysaccharides, bacterial heat shock proteins, bacterial DNA, or saponin based adjuvant molecules. Alternatively, or additionally, one or more cytokines may be co-administered as an adjuvant.

Where the vaccine is based on an isolated nucleic acid sequence, for example a DNA sequence, the nucleic acid may be coated onto minute metal projectiles that can be administered by a ballistic gun technique to penetrate the skin and to permit entry into the muscle beneath. Alternatively, the nucleic acid may be administered in a liposome, and/or in the form of a vector. Such vectors may also encode other factors such as GM-CSF.

The nucleic acid sequences of SEQ.ID.NO:5, SEQ.ID.NO:6, SEO.ID.NO:7 and SEO.ID.NO:8 show the ragB DNA sequences of P. gingivalis. The rag locus of P. gingivalis consists of ragB (encoding an immuno-dominant 55 kDa protein) and a co-transcribed upstream gene, ragA (encoding an 115 kDa outer membrane protein). RagB contains a feature of lipoprotein signal sequence motif and is an important outer membrane protein of P. gingivalis.

Fragments of such sequences may be selected according to their DNA sequence homologues, or the entire sequence may be utilised. Generally, any 18 base-pair fragments will be suitable for generating a 6 amino acid sequence.

One aspect of this invention is therefore to provide a vaccine, which contains all possible RagB antigens (an outer membrane protein of P. gingivalis), which enables the preparation of a host defence for all kind of P. gingivalis, encountered. Such a vaccine composition would be composed of antigenic sequences from all four known pathogenic P. gingivalis strains, W50, QMUL, Thai and 381 as described herein.

In a preferred embodiment of the invention, the vaccine composition, the recombinant polypeptides comprising a a nucleic acid molecule selected from the group consisting of nucleotides of SEQ.ID.NO:5, SEQ.ID.NO:6, SEQ.ID.NO:7 and SEQ.ID.NO:8in any suitable combination and/or orientation, or a fragment of such a nucleic acid molecule.

References to nucleic acid according to the present invention include DNA (genomic DNA as well as cDNA, or antisense DNA) as well as RNA unless the context implies otherwise.

The nucleic acid sequences of the present invention also include sequences that are homologous or complementary to those referred to above. The percent identity of two nucleic acid sequences is determined by aligning the sequences for optimal comparison purposes (e.g., gaps can be introduced in the first sequence for best alignment with the sequence) and comparing the amino acid residues or nucleotides at corresponding positions. The “best alignment” is an alignment of two sequences, which results in the highest percent identity. The percent identity is determined by the number of identical amino acid residues or nucleotides in the sequences being compared (i.e., % identity=# of identical positions/total # of positions×100).

The determination of percent identity between two sequences can be accomplished using a mathematical algorithm known to those of skill in the art. An example of a mathematical algorithm for comparing two sequences is the algorithm of Karlin and Altschul in 1990 (19), modified as in Karlin and Altschul in 1993 (20). The NBLAST and XBLAST programs of Altschul et al (4) have incorporated such an algorithm. BLAST nucleotide searches can be performed with the NBLAST program, score=100, word length=12 to obtain nucleotide sequences homologous to a nucleic acid molecules of the invention. To obtain gapped alignments for comparison purposes, Gapped BLAST can be utilised as described in Altschul et al (5). Alternatively, PSI-Blast can be used to perform an iterated search, which detects distant relationships between molecules (Id.). When utilising BLAST, Gapped BLAST, and PSI-Blast programs, the default parameters of the respective programs (e.g., NBLAST) can be used. See www.ncbi.nlm.nih.gov.

Another example of a mathematical algorithm utilised for the comparison of sequences is the algorithm of Myers and Miller (32). The ALIGN program (version 2.0) which is part of the GCG sequence alignment software package has incorporated such an algorithm. Other algorithms for sequence analysis known in the art include ADVANCE and ADAM as described in Torellis and Robotti (52); and FASTA described in Pearson and Lipman (38). Within FASTA, ktup is a control option that sets the sensitivity and speed of the search.

A nucleic acid sequence which is complementary to a nucleic acid sequence of the present invention is a sequence which hybridises to such a sequence under stringent conditions, or a nucleic acid sequence which is homologous to or would hybridise under stringent conditions to such a sequence but for the degeneracy of the genetic code, or an oligonucleotide sequence specific for any such sequence. The nucleic acid sequences include oligonucleotides composed of nucleotides and also those composed of peptide nucleic acids. Where the nucleic sequence is based on a fragment of the sequences of the invention, the fragment may be at least any ten consecutive nucleotides from the gene, or for example an oligonucleotide composed of from 20, 30, 40, or 50 nucleotides.

Stringent conditions of hybridisation may be characterised by low salt concentrations or high temperature conditions. For example, highly stringent conditions can be defined as being hybridisation to DNA bound to a solid support in 0.5M NaHPO₄, 7% sodium dodecyl sulfate (SDS), 1 mM EDTA at 65° C., and washing in 0.1×SSC/0.1% SDS at 68° C. (Ausubel et al eds. “Current Protocols in Molecular Biology” 1, page 2.10.3, published by Green Publishing Associates, Inc. and John Wiley & Sons, Inc., New York, (1989)). In some circumstances less stringent conditions may be required. As used in the present application, moderately stringent conditions can be defined as comprising washing in 0.2×SSC/0.1% SDS at 42° C. (Ausubel et al (1989) supra). Hybridisation can also be made more stringent by the addition of increasing amounts of formamide to destabilise the hybrid nucleic acid duplex. Thus particular hybridisation conditions can readily be manipulated, and will generally be selected according to the desired results. In general, convenient hybridisation temperatures in the presence of 50% formamide are 42° C. for a probe, which is 95 to 100% homologous to the target DNA, 37° C. for 90 to 95% homology, and 32° C. for 70 to 90% homology.

Examples of preferred nucleic acid sequences for use in according to the various aspects of the present invention are the sequences of the invention are disclosed herein. In particular, the sequences of SEQ.ID.NO:5 and SEQ.ID.NO:6,or a combination of the sequences of SEQ.ID.NO:5, SEQ.ID.NO:6, SEQ.ID.NO:7 and SEQ.ID.NO:8 or fragments thereof. Complementary or homologous sequences may be 75%, 80%, 85%, 90%, 95%, 99% similar to such sequences.

The peptide sequence may be as described above but it also extends to peptides and polypeptides that are substantially homologous thereto. The term “polypeptide” includes both peptide and protein, unless the context specifies otherwise.

Such peptides include analogues, homologues, orthologues, isoforms, derivatives, fusion proteins and proteins with a similar structure or are a related polypeptide as herein defined.

The term “analogue” as used herein refers to a peptide that possesses a similar or identical function as a peptide coded for by a nucleic acid sequence of the invention but need not necessarily comprise an amino acid sequence that is similar or identical to an amino acid sequence of the invention, or possess a structure that is similar or identical to that of a peptide of the invention. As used herein, an amino acid sequence of a peptide is “similar” to that of a peptide of the invention if it satisfies at least one of the following criteria: (a) the peptide has an amino acid sequence that is at least 30% (more preferably, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95% or at least 99%) identical to the amino acid sequence of a peptide of the present invention; (b) the peptide is encoded by a nucleotide sequence that hybridises under stringent conditions to a nucleotide sequence encoding at least 5 amino acid residues (more preferably, at least 10 amino acid residues, at least 15 amino acid residues, at least 20 amino acid residues, at least 25 amino acid residues, at least 40 amino acid residues, at least 50 amino acid residues, at least 60 amino residues, at least 70 amino acid residues, at least 80 amino acid residues, at least 90 amino acid residues, at least 100 amino acid residues, at least 125 amino acid residues, or at least 150 amino acid residues) of a peptide sequence of the invention; or (c) the peptide is encoded by a nucleotide sequence that is at least 30% (more preferably, at least 35%, at least 40%, at least 45%, at least 50%, at least 55%, at least 60%, at least 65%, at least 70%, at least 75%, at least 80%, at least 85%, at least 90%, at least 95% or at least 99%) identical to the nucleotide sequence encoding a peptide of the invention.

As used herein, a peptide with “similar structure” to that of a peptide of the invention refers to a peptide that has a similar secondary, tertiary or quaternary structure as that of a peptide of the invention. The structure of a peptide can determined by methods known to those skilled in the art, including but not limited to, X-ray crystallography, nuclear magnetic resonance, and crystallographic electron microscopy.

The term “fusion protein” as used herein refers to a peptide that comprises (i) an amino acid sequence of a peptide of the invention, a fragment thereof, a related peptide or a fragment thereof and (ii) an amino acid sequence of a heterologous peptide (i.e., not a peptide sequence of the present invention).

The term “homologue” as used herein refers to a peptide that comprises an amino acid sequence similar to that of a protein of the invention but does not necessarily possess a similar or identical function.

The term “orthologue” as used herein refers to a peptide that (i) comprises an amino acid sequence similar to that of a protein of the invention and (ii) possesses a similar or identical function.

The term “related peptide” as used herein refers to a homologue, an analogue, an isoform of, an orthologue, or any combination thereof of a peptide of the invention.

The term “derivative” as used herein refers to a peptide that comprises an amino acid sequence of a peptide of the invention, which has been altered by the introduction of amino acid residue substitutions, deletions or additions. The derivative peptide possesses a similar or identical function as peptides of the invention.

The term “fragment” as used herein with respect to a peptide refers to an amino acid sequence of at least 5 or 6 amino acid residues (preferably, at least 10 amino acid residues, at least 15 amino acid residues, at least 20 amino acid residues, at least 25 amino acid residues, at least 40 amino acid residues, at least 50 amino acid residues, at least 60 amino residues, at least 70 amino acid residues, at least 80 amino acid residues, at least 90 amino acid residues, at least 100 amino acid residues) of the amino acid sequence of a peptide of the invention. Fragments of nucleic acid sequences may be defined correspondingly.

The term “isoform” as used herein refers to variants of a peptide that are encoded by the same gene, but that differ in their isoelectric point (pI) or molecular weight (MW), or both. Such isoforms can differ in their amino acid composition (e.g. as a result of alternative splicing or limited proteolysis) and in addition, or in the alternative, may arise from differential post-translational modification (e.g., glycosylation, acylation, phosphorylation). As used herein, the term “isoform” also refers to a protein that peptide exists in only a single form, i.e., it is not expressed as several variants.

The skilled person is aware that various amino acids have similar properties. One or more such amino acids of a substance can often be substituted by one or more other such amino acids without eliminating a desired activity of that substance. Thus the amino acids glycine, alanine, valine, leucine and isoleucine can often be substituted for one another (amino acids having aliphatic side chains). Of these possible substitutions it is preferred that glycine and alanine are used to substitute for one another (since they have relatively short side chains) and that valine, leucine and isoleucine are used to substitute for one another (since they have larger aliphatic side chains which are hydrophobic). Other amino acids which can often be substituted for one another include: phenylalanine, tyrosine and tryptophan (amino acids having aromatic side chains); lysine, arginine and histidine (amino acids having basic side chains); aspartate and glutamate (amino acids having acidic side chains); asparagine and glutamine (amino acids having amide side chains); and cysteine and methionine (amino acids having sulphur containing side chains). Substitutions of this nature are often referred to as “conservative” or “semi-conservative” amino acid substitutions.

Amino acid deletions or insertions may also be made relative to the amino acid sequence of a peptide sequence of the invention. Thus, for example, amino acids which do not have a substantial effect on the biological activity or immunogenicity of such peptides, or at least which do not eliminate such activity, may be deleted. Amino acid insertions relative to the sequence of peptides of the invention can also be made. This may be done to alter the properties of a peptide of the present invention (e.g. to assist in identification, purification or expression. Such amino acid changes relative to the sequence of a polypeptide of the invention from a recombinant source can be made using any suitable technique e.g. by using site-directed mutagenesis.

A nucleic acid construct according to the invention may suitably be inserted into a vector, which is an expression vector that contains nucleic acid sequences as defined above. The term “vector” or “expression vector” generally refers to any nucleic acid vector, which may be RNA, DNA or cDNA.

The term “expression vector” may include, among others, chromosomal, episomal, and virus-derived vectors, for example, vectors derived from bacterial plasmids, from bacteriophage, from transposons, from yeast episomes, from insertion elements, from yeast chromosomal elements, from viruses such as baculoviruses, papova viruses, such as SV40, vaccinia viruses, adenoviruses, fowl pox viruses, pseudorabies viruses and retroviruses, and vectors derived from combinations thereof, such as those derived from plasmid and bacteriophage genetic elements, such as cosmids and phagemids. Generally, any vector suitable to maintain, propagate or express nucleic acid to express a polypeptide in a host may be used for expression in this regard. The vector may be constructed from a bacterial plasmid, for example the bacterial plasmid pUC18.

Recombinant expression vectors will include, for example, origins of replication, a promoter preferably derived from a highly expressed gene to direct transcription of a structural sequence as defined above, and a selectable marker to permit isolation of vector containing cells after exposure to the vector.

Expression vectors may comprise an origin of replication, a suitable promoter as defined herein and/or enhancers, and also any necessary ribosome binding sites, polyadenylation regions, splice donor and acceptor sites, transcriptional termination sequences, and 5′-flanking non-transcribed sequences that are necessary for expression. Preferred expression vectors according to the present invention may be devoid of enhancer elements. The expression vectors may also include selectable markers, such as antibiotic resistance, which enable the vectors to be propagated.

Introduction of an expression vector into the host cell can be effected by calcium phosphate transfection, DEAE-dextran mediated transfection, microinjection, cationic lipid-mediated transfection, electroporation, transduction, scrape loading, ballistic introduction, infection of other methods. Such methods are described in many standard laboratory manuals, such as Sambrook et al., Molecular Cloning: A Laboratory Manual, 2^(nd) Ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (1989).

In certain embodiments of the invention, the vectors may provide for specific expression. Such specific expression may be inducible expression or expression only in certain types of cells or both inducible and cell-specific. Preferred among inducible vectors are vectors that can be induced for expression by environmental factors that are easy to manipulate, such as temperature, nutrient additives, hypoxia and/or the presence of cytokines or other biologically active factors. Particularly preferred among inducible vectors are vectors that can be induced for expression by changes in the levels of chemicals, for example, chemical additives such as antibiotics. A variety of vectors suitable for use in the invention, including constitutive and inducible expression vectors for use in prokaryotic and eukaryotic hosts, are well known and employed routinely by those skilled in the art.

The promoter sequence may be any suitable known promoter, for example the human cytomegalovirus (CMV) promoter, the CMV immediate early promoter, the HSV thymidine kinase promoter, the early and late SV40 promoters or the promoters of retroviral LTR's, such as those of the Rous sarcoma virus (“RSV”), and metallothionein promoters, such as the mouse metallothionein-I promoter. The promoter may comprise the minimum sequence required for promoter activity (such as a TATA box without enhancer elements), for example, the minimal sequence of the CMV promoter (mCMV). Preferably the promoter is a mammalian promoter that can function at a low basal level devoid of an enhancer element.

The DNA comprising the nucleic acid sequence of the invention may be single or double stranded. Single stranded DNA may be the coding or sense strand, or it may be the non-coding or anti-sense strand. For therapeutic use, the nucleic acid sequences are in a form capable of being expressed in the subject to be treated.

The termination sequences in the vector may be a sequence of adenylate nucleotides, which encode a polyadenylation signal. Typically, the polyadenylation signal is recognisable in the subject to be treated, such as, for example, the corresponding sequences from viruses such as, for human treatment, and the SV40 virus. Other termination signals are well known in the art and may be used.

Preferably, the polyadenylation signal is a bi-directional terminator of RNA transcription. The termination signal may be the polyadenylation signal of the simian 40 virus (SV40), for example the SV40 late poly(A). Alternatively, the termination sequence may be the polyadenylation signal of bovine growth hormone which results in maximal expression when combined with a CMV promoter (54).

According to a second aspect of the invention, there is provided a vaccine composition comprising a polypeptide encoded by a nucleic acid molecule having a nucleic acid sequence of SEQ.ID.NO:5, SEQ.ID.NO:6, SEQ.ID.NO:7 or SEQ.ID.NO:8or a fragment thereof.

Fragments of such sequences may be selected according to their antigenic determinants, or the entire sequence may be utilised. Generally, 6 amino acid sequences that form an epitope will be suitable.

According to a third aspect of the invention, there is provided an antibody composition, the composition comprising at least one antibody raised against the recombinant polypeptide composition as first aspect of the invention, wherein the antibody specifically binds a polypeptide having a sequence selected from the group consisting of residues 1-505of SEQ.ID.NO:9 (QMLRagB), residues 1-501 of SEQ.ID.NO:10 (ThaiRagB), 501 of SEQ.ID.NO:11 (W50RagB) and residues 1-505 of SEQ.ID.NO:12 (381RagB).

According to a fourth aspect of the invention, there is provided a polypeptide having a sequence selected from the group consisting of residues 1-505 of SEQ.ID.NO:9(QMLRagB), residues 1-501 of SEQ.ID.NO:10 (ThaiRagB), 501 of SEQ.ID.NO:11(W50RagB) and residues 1-505 of SEQ.ID.NO:12 (381RagB) for use in medicine.

Uses in accordance with these aspects of the invention that are directed to treatment or prevention of disease caused by P. gingivalis, therefore also extend to methods of treatment for such conditions or diseases, the methods comprising the administration to a subject a vaccine composition of the invention as described above.

As part of such methods, it may be convenient to determine which strain of P. gingivalis is the infectious agent in order to be able to specifically select a vaccine directed against the correct allele of RagB. Whilst all 4 variant strains can be targeted, it is more effective and cheaper to target the actual infectious agent present in a patient by means of a pre-treatment diagnostic step.

According to an eighth aspect of the invention, there is provided an oral healthcare composition, which comprises a vaccine in accordance with other aspects of the invention described above.

Such oral healthcare compositions may be, but are not limited to pastes (e.g. toothpastes), mouthwashes, gum (e.g. a confectionery based chewing gum, preferably sugar-free).

Vaccine compositions may also be used to coat oral healthcare implements or instruments, e.g. dental floss or tape, etc.

The present invention therefore also includes such antibodies for use in medicine, and the use of the antibodies in the preparation of a medicament for the treatment or prevention of periodontitis, or of infection of a subject by P. gingivalis. Methods of treatment as described above therefore also include the administration of such antibodies as part of a method of immunotherapy for the treatment or prevention of such diseases.

The nucleic acid sequences of the present invention may also be used to screen samples for the presence of P. gingivalis. Accordingly, the present invention additionally provides kits for the detection of P. gingivalis in a sample in which the kit comprises specifically designed primers for use in a DNA amplification procedure, such as the Polymerase Chain Reaction (PCR). Suitably, such kits are provided with instructions for use in the detection of the presence of P. gingivalis in a sample, or a method for the diagnosis of such an infection in a subject. Alternatively, the antibodies of the present invention can be used as the basis of a kit for the detection of P. gingivalis in a sample from a patient. Detection of the antigen can be accomplished by any suitable means for the detection of antigen-antibody binding, such as ELISA, radio-immunoassay, etc.

The vaccine compositions of the present invention also provide the basis for novel and effective combination therapies to treat or prevent periodontitis or infection of a subject by P. gingivitis. Such methods of treatment may comprise the separates sequential or simultaneous administration to a subject of a vaccine composition of the invention and another pharmaceutical substance, such as an antibiotic or an antimicrobial agent.

Suitable antibiotics may include, but are not limited to, metronidazole, clindamycin, or ciprofloxacin. Suitable, antimicrobial agents may include, but are not limited to, triclosan, chlorhexidine or sodium hypochlorite.

Preferred features for the second and subsequent aspects of the invention are as for the first aspect mutatis mutandis.

The present invention will now be described by way of further example with reference to the following Examples and drawings, which are included for the purposes of illustration only and are not to be taken as being limiting on the invention.

Brief description of drawings is listed below:

FIG. 1 shows the nucleic acid sequence of SEQ.ID.NO:1 for ragB allele QML (ragB3).

FIG. 2 shows the nucleic acid sequence of SEQ.ID.NO:2 for ragB allele Thai (ragB2).

FIG. 3 shows the nucleic acid sequence of SEQ.ID.NO:3 for ragB allele W50(ragB1).

FIG. 4 shows the nucleic acid sequence of SEQ.ID.NO:1 for ragB allele 381(ragB4).

FIG. 5 shows the nucleic acid sequence alignments for ragB alleles SEQ.ID.NO:5 to SEQ.ID.NO:8.

FIG. 6 shows the amino acid sequence alignments for RagB alleles SEQ.ID.NO:9to SEQ.ID.NO:12.

FIG. 7 shows the rag locus in P. gingivalis W83 in diagrammatical form with primer details.

Primers designed for the rag locus: Forward (orf2 6586-6606), SEQ.ID.NO:15, 5′-CAAAGTCCTGCCACGAGTAGC-3 ′; Reverse (orfV 388-408), SEQ.ID.NO:16, 5′-CGITITCTCGCCACTTTCGTC-3′.

FIG. 8 shows the results of PCR amplification of rag locus and digestion with HaeIII. FIG. 8( a) shows the rag locus size different; FIG. 8( b) shows the restriction map patterns are different.

FIG. 9 shows the results of a sequence comparison of rag locus from the four main groups found in patient samples.

FIG. 10 shows the results of a Western blot assay conducted on cell lysates from four strains of different ragB alleles react with anti-P. gingivalis W50 RagB antibodies. “A” shows blot with monoclonal antibody against recombinant W50 RagB (1B15/31). “B” shows blots with polyclonal antibody against recombinant W50 RagB (02NH); No cross-reactions observed among four groups of RagB.

FIG. 11 shows in diagrammatic form of the four different ragB alleles with primer design (specific primers were designed for each group).

FIG. 12 shows the results of multiplex-PCR detection of ragB alleles. There is only one specific band for individual isolate of P. gingivalis.

FIG. 13 shows the construction of ragA mutant in P. gingivalis W50 (JMA1) in FIG. 13( a); FIG. 13( b) shows Southern blot, ragA as a probe; FIG. 13( c) shows check ragA mutation using PCR with ragA primers.

FIG. 14 shows the characterisation of ragA mutant (JMA1) in SDS-PAGE and Western blot. 12.5% SDS-PAGE and Western blot analysis of P. gingivalis W50 and mutant strain cells. FIG. 14( a) shows stain with Coomassie blue (ragA-lost bands at 115 kDa and 55 kDa). FIG. 14( b) shows blots react with anti-RagB antibody (E38). Rag B also absent in ragA-.

FIG. 15 shows a virulence study of P. gingivalis and ragA mutant in the mouse animal model.

FIG. 16 shows the construction of ragB into expression vector (His6-RagB pNY34). RagB was synthesised with His₆ tag, minus the first 23 amino acid putative signal peptide sequence, under the control of tac promoter and IPTG induction in E. coli XL1 Blue. The expected size of the recombinant protein was 55.7 kDa.

FIG. 17 shows the purification of recombinant RagB of P. gingivalis. Elute recombinant RagB from Ni-NTA column.

FIG. 18 shows animals' immune response to recombinant RagB. Antibody titre detection by using ELISA (coated with recombinant RagB)—1:12800 dilution. Mice immunized with recombinant RagB W50 and immune response was tested. Specific antibody against recombinant RagB was detected at a very high level.

FIG. 19 shows the protection of mice from lesion formation when challenged with P. gingivalis W50.

FIG. 20 shows the protection effect of immunisation basis on survival time. Immunized mice showed a longer survival time than non-immunized mice post challenge of P. gingivalis W50 at the dose (M=10⁹ cfu/mouse).

EXAMPLE 1 Heterogeneity in the Rag Locus of P. gingivalis

Materials and Methods:

Bacterial Strains and Culture Conditions

Isolates were grown on Fastidious Anaerobic Agar (FAA) plates with 5% defibrinated horse blood, or Brain Heart Infusion (BHI) broth with 5 μg ml⁻¹ haemin at 37° C. in an anaerobic cabinet (Don Whitley Scientific) with an atmosphere of 80% N₂, 10% H₂, 10% CO₂

A total of 168 isolates of P. gingivalis from the laboratory collection of the inventors were investigated, including isolates generously supplied by numerous colleagues of the inventors. All isolates had been recovered from human sources, mostly from patients with periodontal disease, and were from 15 countries. Isolates were confirmed to be P. gingivalis by PCR with species-specific primers to 16S rRNA genes.

DNA Manipulations

Total genomic DNA was isolated from stationary phase bacteria using a Puregene DNA isolation kit reagent (Flowgen) under manufacturer's instructions. Briefly, 1 ml of overnight BHI cultures was lysed with 600 μl cell lysis solution at 80° C. for 5 minutes. Cells were treated with 3 μl RNaseA solution at 37° C. for 1 hour. Protein was removed by precipitation with guanidine thiocyanate and the DNA was precipitated and cleaned with successive washes of 100% isopropanol and 70% ethanol. Purified DNA was resuspended in 50 μl TE (10 mM Tris, 1 mM EDTA, pH 8.0).

DNA purification to remove primers, enzymes and other reagents was undertaken using a Qiagen Gel Extraction Kit. Briefly, DNA was bound to a silicon based ion exchange matrix under high salt conditions in buffer PB. The DNA was cleaned with two washes of buffer PE and eluted in 50 μl TE.

Restriction digestion of PCR products was performed using Amersham Pharmacia or New England Biolabs enzymes and buffers. Reactions were incubated at 37° C. for at least 2 hours. DNA electrophoresis was performed in 0.8% agarose with Tris-Borate-EDTA (0.09M Tris-borate, 0.002M EDTA). Ethidium bromide stained gels were viewed under UV light and the image captured.

The primers designed to be specific to P. gingivalis:

16s rRNA, SEQ.ID.NO: 13, Forward primer: 5′- AGG CAG CTT GCC ATA CTG CG -3′ SEQ.ID.NO: 14, Reverse primer: 5′- ACT GTT AGC AAC TAC CGA TGT -3′ rag locus, SEQ.ID.NO: 15, Forward primer: 5′- CAAAGTCCTGCCACGAGTAGC -3′ SEQ.ID.NO: 16, Reverse primer: 5′-CGTTTTCTCGCCACTTTCGTC-3′ rag1 (W50), SEQ.ID.NO: 17, Forward primer: 5′-CGC GAC CCC GAA GGA AAA GAT T-3′ SEQ.ID.NO: 18, Reverse primer: 5′-CAC GGC TCA CAT AAA GAA CGC T-3′ rag2 (Thai), SEQ.ID.NO: 19, Forward primer: 5′-GCT TTG CCG CTT GTG ACT TGG-3′ SEQ.ID.NO: 20, Reverse primer: 5′-CCA CCG TCA CCG TTC ACC TTG-3′ rag3 (QML), SEQ.ID.NO: 21, Forward primer: 5′-CCG GAA GAT AAG GCC AAG AAA GA-3′ SEQ.ID.NO: 22, Reverse primer: 5′-ACG CCA ATT CGC CAA AGC T-3′ rag4 (381), SEQ.ID.NO: 23, Forward primer: 5′-CCG GAT GGA AGT GAT GAA CAG A-3′ SEQ.ID.NO: 24, Reverse primer: 5′-CGC GGT AAA CCT CAG CAA ATT-3′ Polymerase Chain Reaction (PCR)

All amplification reactions were performed in a PCR thermal cycler. Standard PCR reactions used 50 μl volumes with 0.5μg each primer and 0.5 μl chromosomal DNA template in a PCR buffer with 1.5 mM MgCl₂. Amplification of longer products was performed Standard programs for PCR comprised 25 cycles of denaturation 1 minute at 95° C., annealing 1 minute at 50° C., and extension 1-3 minutes at 72° C. For long PCR, 10 cycles with annealing at 52° C. and an extension time of 6 minutes 40 sec at 68° C. were followed by 15 cycles with annealing at 60° C. and 7 minutes extension at 68° C.

SDS-PAGE and Western Blotting

SDS-PAGE was performed according to the method of Laemmli on 12% separating gels. Briefly, samples were prepared from 1.5 ml original culture volumes. Cell pellets were resuspended in 135 μl of 0.2% SDS and whirly mixed; protease inhibitor leupeptin was added to a final concentration of 100 μg/ml and incubated at room temperature for 10 minutes. The inactivated sample was then diluted 1:1 in working strength sample buffer (2×SDS) and heated at 100° C. for 5 minutes. Samples (10 μl equivalent to 50 μl of the original culture) were loaded 10 μl per lane. Western blotting was carried out in a bicarbonate transfer buffer (3 mM Na₂CO₃, 10 mM NaHCO₃, pH 9.9, 20% [vol/vol] methanol) at a constant current of 400 mA for 1 hour using nitrocellulose membranes. After blotting, the membranes were blocked in 5% bovine serum albumin and incubated overnight in B15 and O2NH anti-recombinant RagB antibodies. Antibody binding was detected by using HRP-conjugated anti-mouse and anti-rabbit immunoglobulins (Dako, Germany).

DNA Sequence Determination and Nucleotide Sequence Accession Numbers

Long PCR products from Thai (A011/9), QML (QM220), and 381 (strain obtained as ATCC33277^(T)) were purified and sent to MWG-Biotech for sequence determination, using their publication grade sequencing service. Open reading frames were identified with FramePlot 2.3.2 online software. The nucleotide sequence data reported in this study have been assigned GenBank accession numbers AY842852 (381), AY842853 (QML) and AY842854 (That).

Summary: Following analysis of the restriction enzyme map pattern of rag locus (see FIGS. 7 and 9), it was found that ragB apparently appeared in four main groups and these four-ragB gene alleles from different groups were sequenced (see FIGS. 1-4). There is a high DNA variation between them, their similarity around about 60% as well as protein sequence (see FIGS. 5-6 and 8). The specific primers were designed for each group. A multiple-PCR method was employed to identify ragB alleles from P. gingivalis collections. Local clinical samples and isolates of P. gingivalis from a worldwide collection were tested to obtain information of P. gingivalis in clinical population for ragB in different strains of P. gingivalis. The results showed that majority (97%) of clinical samples contained just a single PCR product specific for one of the four groups (see FIGS. 11-12). Furthermore, the results from western blot indicated that antibodies against P. gingivalis W50 RagB do not cross-react with other RagB groups (see FIG. 10). These findings confirmed that ragB gene is divided into four major sequence and antigenic groups.

EXAMPLE 2 The Role of the Rag Locus of P. gingivalis W50 in Virulence

Materials and Methods:

Bacterial Strains, Plasmid, and Culture Conditions

P. gingivalis W50 were used as standard reference strain in this study. Culture conditions for P. gingivalis have been described in the example 1. Plasmid pVA2198, which carries a copy of ermF-ermAM (erm) cassette, has been described previously and was used to provide Clindamycin resistant marker for mutagenesis. Clindamycin was used at 5 μg/ml.

PCR and DNA Manipulations

Primers designed to amplify ragA from P. gingivalis W50 genomic DNA were: forward primer, SEQ.ID.NO:25, 5′-CGCTATTCTTCCTTTGCTTGCT-3′, reverse primer, SEQ.ID.NO:26, 5′-TTACCATCCGCATCGACTTGA-3′. PCR amplification was performed with Techne's thermal Cycler in reaction mixtures (50 μl) containing 60 μM of each primer, 50 ng of template DNA, and 45 μl of PCR master mix (Abgene, Surrey, UK). The PCR consisted of 25 cycles with a temperature profile of 1 minute at 95° C., 1 minute at 50° C., and 3 minutes at 72° C., followed by 1 cycle of 7 minutes at 72° C. The amplified DNAs were analysed in 0.7% agarose-TBE gel. The specific PCR products of 3.0-kb ragA were digested with SacI and PstI consecutively; prospective DNA fragments were purified and ligated with erm cassette (SacI/PstI) cut from plasmid DNA pVA2198 (7). The primers used for amplification of ragA gene were employed to amplify the ligations to ensure that a reconstructed product, ragA::erm, was in the mixture. This methodology led to the construct with a deletion of 1.5 kb in ragA replaced with a 2.1 kb erm; the interrupted gene is now 600 bp bigger than the original ragA (see FIG. 13).

Construction of Allelic-Exchange Mutant

The amplicons (from above) were used to generate P. gingivalis JMA1 (ragA::erm). The constructs were transformed into competent cells of P. gingivalis W50 by electroporation. Briefly, 1 ml of an actively growing culture of P. gingivalis was used to inoculate 10 ml of BHI broth supplemented with hemin and menadione, and then was incubated overnight at 37° C. The overnight culture was then inoculated into 30 ml of fresh pre-warmed BHI at 1:10 dilution and then grown for 6 hr. The culture of P. gingivalis was harvested by centrifugation at 10,000 (g) for 10 min at 4° C. and washed in 30 ml of electroporation buffer (EPB; 10% glycerol, 1 mM MgCl₂; filter sterilized; stored at 4° C.), and the pellet was suspended in 600 μl EPB. Approximately 200 ng of DNA was added to 200 μl cells in a 0.2 cm-path length cuvette. The cells were pulsed with a Bio-Rad Gene Pulser at 2.5 kV for the potential difference, 200Ω for the resistance and 25 μF for the capacitance. P. gingivalis cells were then immediately diluted in 1 ml BHI-haemin broth (at room temperature) and allowed to recover for 16 hr in the anaerobic cabinet. After overnight recovery, initial selection of mutants was performed on blood agar plates containing Clindamycin (5 μg/ml) and incubated anaerobically at 37° C. for 7 to 10 days. Following allelic exchange mutagenesis, mutants in each category were characterized by phenotypic analysis.

SDS-PAGE and Western Blotting

Preparation of extracts described in example 1. Samples electrophoresis on 10% polyacrylamide gels, and the gel was stained with Coomassie blue (see FIG. 14). Detection of the 55 kDa outer membrane antigen RagB with monoclonal antibody E38 was performed (see FIG. 14).

Southern Blotting

Genomic DNAs were digested with the appropriate restriction endonucleases and electrophoresed in agarose gels, and then transferred onto Hybond N+ membranes. The membranes were prehybridized for 1 hour at 65° C. in a hybridisation buffer and hybridised overnight in the same solution with dig-labelled probes. The probe DNA for ragA was prepared by PCR, and that for erm was prepared by EcoRI and SphI restriction digestion of plasmid pVA2198. The probes were labelled by the random-primer method with digoxigenin-dUTP following the manufacturer's instructions. Detection of hybrids was performed by enzyme immunoassay.

Murine Virulence Model Protocols

The virulence potentials of P. gingivalis W50 and JMA1 (ragA::erm) were examined by using the murine lesion model. Briefly, bacterial cells from an 18-hour culture in BHI medium (containing 5 μg/ml of hemin) were harvested by centrifugation and resuspended to a final density in the culture medium at the required concentration for inoculation into the mice. Groups of BALB/c mice (8 per group) were inoculated subcutaneously twice with 100 μl portions of bacterial cell suspensions on the mid point of each flank towards the dorsal surface. Three bacterial doses were employed at 1×10¹¹, 5×10¹⁰ and 2.5×10¹⁰ cfu/ml in each group. The animals were then monitored twice daily for 8 days for the development of lesions and to assess their general condition according to a standardized appearance and behaviour scoring system which was approved by the local ethics committee and the United Kingdom Home Office animal experimentation licensing authority.

Summary: To investigate the role of the rag locus of P. gingivalis W50 in virulence, an isogenic ragA mutant with expresses neither RagA nor RagB was constructed following PCR, insertion of an Erm cassette in vitro, and electro transformation with the construct. The mutant, JMA1, was confirmed by PCR, Southern hybridisation, SDS-PAGE, and Western blotting (see FIGS. 13-14). JMA1 was used in a murine model for virulence investigation. Groups of mice (8 mice/group) were subcutaneously inoculated with 5×10⁹-2×10¹⁰ cfu of P. gingivalis/mouse and their size, weight, behaviour and appearance over 8 days were monitored. Results showed that inactivation of ragA lead to a significant reduction (P<0.001) in the virulence of P. gingivalis W50 at 5×10⁹ and 10¹⁰ cfu/mouse on the basis of time of survival (see FIG. 15). These data suggest that the rag locus of P. gingivalis W50 plays an important role in the virulence of this strain.

EXAMPLE 3 Cloning and Expression of RagB of P. gingivalis in E. coli

Materials and Methods:

Bacteria and Growth Conditions

Culture conditions for P. gingivalis described in example 1. Escherichia coli XL-1 Blue (Stratagene) were grown in Luria-Bertani medium.

Primers

Primers designed to amplify the ragB of P. gingivalis W50 were:

SEQ.ID.NO: 27, RagBF1: 5′-ATATATGAGCTCCGCGACCCCGAAGGAAAAG-3′ SEQ.ID.NO: 28, RagBRI: 5′-TATATAGTCGACGAAAAGATAGGGGCTGCGAC-3′ the italicized sequences represent SacI and SalI sites, respectively, were designed to generate the cloning sites. PCR

PCR were performed for 25 cycles, and the parameters were: denaturation, 94° C., 1 min; annealing, 60° C., 1 min; extension, 72° C., 4 min.

Clone RagB into Fusion Protein Expression Vector

The 1,508-bp partial SstI-SalI amplicon was subsequently cloned into the corresponding sites in pJFQ3010, a derivative of pQE30 (7), to generate NY34 as a (His)6-tagged recombinant protein.

The recombinant plasmid was then propagated in Escherichia coli XL-1 Blue with selection for ampicillin resistance. This scheme ensured that RagB, minus the first 23-amino-acid putative signal peptide sequence, was synthesized as an N-terminal His6 fusion protein under the control of the tac promoter and IPTG (isopropyl-β-D-thioga-lactopyranoside) induction in E. coli XL-1 Blue. The predicted size of the recombinant protein was 55.7 kDa (see FIG. 16).

Purification of Recombinant Proteins

E. coli XL-1 Blue was transformed with the appropriate expression construct and grown overnight at 37° C. in Luria-Bertani medium incorporating ampicillin at 50 μg/ml. Cells were harvested by centrifugation and solubilized in 0.01 M imidazole lysis buffer (Phosphate buffer, 8M Urea or 6M Guanidine HCl pH8). Supernatant from the lysate was incubated for 1 hour at room temperature with Ni-nitrilotriacetic acid agarose (Qiagen) and packed into a column, which was first washed with lysis buffer containing 0.02 M imidazole pH6.3 and eluted with 0.25 M imidazole in lysis buffer pH5.9 (see FIG. 17). The eluted protein was dialyzed against 0.15 M saline, filter sterilized. The identities of the recombinant proteins were confirmed by SDS-PAGE and Coomassie blue stain. The concentration of the recombinant protein was examined. The recombinant proteins were then stored at minus 20° C.

Summary: ragB has been successfully cloned from genomic DNA of P. gingivalis W50 and P. gingivalis Thai strains (data not shown) according sequence data.

The ragBs were constructed into pQE expression vectors and the recombinants were expressed in E. coli XL-1 Blue. To purify recombinant RagB, Ni-NTA metal-affinity chromatography column was employed. It was found that the use of poly-His fusion expression system can make an efficient amount of protein for immunisation in an animal model.

EXAMPLE 4 Host Immune Response Following Immunization with P. gingivalis W50 RagB

Materials and Methods:

Preparation of Immunogens

The adjuvant used for this study was Aluminum Hydroxide. Fresh made Al(OH)₃ was mixed with recombinant RagB. Briefly, 10 ml of 10% potassium alum (aluminum potassium sulfate, AlK(SO4)₂.12H₂O) in a 50-ml conical tube, vortex and add 22.8 ml of 0.25N NaOH dropwise; centrifuge at 1000 g for 10 minutes after incubation at room temperature for 10 minutes; wash the pellet with distilled water. 1 mg of Al(OH)₃ can bind approximately 50-200 μg of protein antigen. The adjuvant and the recombinant RagB were incubated in 0.9% saline at room temperature for 20 minutes. Spin at 10,000 g for 10 minutes. Test the supernatant for the presence of the antigen to calculate the amount of antigen bound to the adjuvant.

Immunisation

5-week-old BALB/c mice purchased from an approved supplier and allowed 1-week acclimatisation. Animals were inoculated subcutaneously with ˜25 μg protein (RagB)/adjuvant in 100 μl. A booster injection was given 4 weeks later with the same amount and volume of immunogen-emulsified adjuvant. Four weeks later blood samples were taken to assay for antibodies.

Collection of Sera and Determination of Antibody Titre

15-50 μl of blood sample was taken from mice. Incubate the blood samples for 60 minutes at 37° C. to allow complete coagulation and clot reaction. Centrifuge blood samples at 10,000 g for 10 minutes to separate sera from blood cells after overnight incubation at 4° C. The sera were stored frozen (−20° C.). ELISA and Western blot were employed to detect the antibodies against recombinant RagB and native RagB. If the titre is not satisfactory at this step, another boost injection may be required.

Summary: The immune response of mice immunized with recombinant RagB of P. gingivalis W50 was examined and it was found that all immunised animals produced a high antibody titre against the recombinant protein itself and the native protein of RagB from this organism (see FIG. 18).

EXAMPLE 5 Investigation of Protection Offered Following Challenge

Materials and Methods,

Animals:

48 BALB/c mice immunised with recombinant RagB were split into six groups. Each group had same number of non-immunization mice as age-control.

Challenge Experiment

The murine lesion model used for virulence study has been described in example 2. Briefly, bacterial cells from an 18-h culture in BHI medium (containing 5 μg/ml of hemin) were harvested by centrifugation and resuspended to a final density in the culture medium at the required concentration. Groups of BALB/c mice (8 per group) both immunised and non-immunised were inoculated subcutaneously twice with 100 μl portions of bacterial cell suspensions on the mid point of each flank towards the dorsal surface. Five bacterial doses of P. gingivalis W50 were inoculated at 4×10¹¹, 2×10¹¹, 10¹⁰, 5×10⁹ and 2.5×10⁹ cfu/ml; 10¹⁰) cfu/ml of P. gingivalis Thai. The animals were then monitored twice daily for 8 days for the development of lesions and to assess their general condition according to a standardized appearance and behaviour scoring system.

Summary: The protective effect of immunisation with recombinant RagB was evaluated in the same animal model described above. The results showed that immunisation protected animals from subcutaneous challenge with the homologous strain based on lesion size and survival time (see FIGS. 19-20). The cross reactivity was tested of sera from animals immunised with recombinant RagB from P. gingivalis W50 with other P. gingivalis strains carrying one of the three alternative rag alleles. No cross-reaction was observed between P. gingivalis W50 and P. gingivalis Thai on the basis of Western blotting (see FIG. 10). Hence, it is considered unlikely that there will be any cross-protection in mice immunised with RagB from W50 and challenged with P. gingivalis carrying alternative RagB alleles. This was confirmed in preliminary experiments, which showed that immunisation with recombinant RagB from P. gingivalis W50 (ragB1 group) did not protect animals challenged with P. gingivalis Thai strain (ragB2 group). The data therefore indicates that RagB is a promising vaccine candidate.

EXAMPLE 6 Mixture of Recombinant Proteins

-   -   1. Based on the outcome of the protection experiments, a         recombinant protein mixture will be used as the immunogen in the         immunisation/challenge experiment. The whole procedure will be         similar to the experiments described before but a mixture of         proteins in a 1:1:1:1 ratio will instead of single allelic         recombinant protein.     -   2. 96 mice in 12 groups will be immunized with the emulsion         mixture and boosted as described above.     -   3. One week after final boost, both immunized and non-immunized         mice will be subcutaneously inoculated with 5×10⁹-2×10¹⁰ cfu         of P. gingivalis from the four major allelic type of ragB per         mouse and their lesion size, weight, behaviour and appearance         over 8 days will be monitored.

EXAMPLE 7 Engineering Recombinant Streptococcus gordonii Expressing P. gingivalis RagB Domains

-   -   1. Design specific primers with suitable restriction enzyme cut         site at both ends for ragB in each group. PCR will be employed         to amplify ragB from different groups.     -   2. Clone ragB into insertion vector pSMB55 to obtain         translational gene fusions. The resulting chimeric plasmid will         be used to transform S. gordonii. The transformants will be         selected on plates containing erythromycin.     -   3. The recombinant colonies will be then confirmed by PCR and         Southern blot hybridisation. The expression of RagB will be         tested on SDS-PAGE followed by immunoblotting analysis. The         positive colonies can be freezing dried or stored at −70° C.     -   4. Experimental animals (mice and/or rabbits) will be used to         examine the immunogenicity of RagB from the recombinant S.         gordonii. The animals will be immunized subcutaneously with 10⁹         live S. gordonii cells emulsified in a copolymer adjuvant. The         antibodies in the sera of immunized animals will be tested by         ELISA and immunoblotting against P. gingivalis RagB.     -   5. To test oral colonization and immune response, Sprague-Dawley         germfree rats will be used as a model. The recombinant S.         gordonii will be administrated into the oral cavity (10⁹ cfu)         two inoculations 24 h apart. To assess S. gordonii colonization,         oral swabs will be taken at regular weekly intervals. Immune         response and prevention will be tested as described above.

EXAMPLE 8 Determine the Potential Protective Effect of Specific Antibodies in a P. gingivalis Challenge Model

-   -   1. Suspensions of freshly harvested bacterial cells are adjusted         to the required cell density (e.g. for P. gingivalis W50:5×10⁹         cfu/ml).     -   2. Adult mice (6-10 weeks old) are separated into six groups (8         mice/group) and marked so they are individually identifiable.     -   3. Group 1 as a positive control receive P. gingivalis; group 2         for testing prevention effect of passive antibody transfer         receive specific antibody 24 hours prior to P. gingivalis         challenge; group 3 same as group 2 but irrelevant Ig instead of         specific antibody for passive antibody transfer negative         control; group 4 receive P. gingivalis opsonized with specific         antibody; group 5 receive P. gingivalis opsonized irrelevant Ig         for opsonization negative control; group 6 a negative control         receive BHI broth only.     -   4. The prepared cell suspension will be inoculated into groups         of mice for challenge experiments. The animals are inoculated         subcutaneously with 0.1 ml of bacterial suspension at an         appropriate dose at a site midway down each flank.     -   5. Following challenge, each animal is examined daily for signs         of infection and to assess its' general condition.     -   6. After 15 days, or at the time of killing, localised or         spreading lesion size (length and width) is measured with a         caliper, the area determined and expressed in square         millimeters.

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1. An immunogenic composition comprising the nucleic acid molecules of nucleotides 1-1518 of SEQ.ID.NO:5(QMLragB), nucleotides 1-1506 of SEQ.ID.NO:6 (ThairagB) and nucleotides 1-1518 of SEQ.ID.NO:8 (381ragB), wherein the nucleic acid molecules SEQ.ID.NO:5, SEQ.ID.NO:6 and SEQ.ID.NO: 8 encode a polypeptide SEQ.ID.NO: 9, SEQ.ID.NO: 10 and SEQ.ID.NO: 12 respectively.
 2. An oral healthcare composition comprising a composition as in claim
 1. 3. A kit for the detection of P. gingivalis in a sample comprising one or more probes consisting of 19-23 nucleotides from 1-1518 of SEQ.ID.NO:5 (QMLragB), 1-1506 of SEQ.ID.NO:6 (ThairagB)and 1-1518 of SEQ.ID.NO:8 (381ragB). 